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1. |
Acidic Fibroblast Growth Factor (aFGF) in Developing Normal and Dystrophic (mdx) Mouse Muscles. Distribution in Degenerating and Regenerating mdx Myofibres |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 97-106
OliverLisa,
RaulaisDaniel,
VignyMarc,
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摘要:
AbstractAffinity purified polyclonal antibodies directed against human recombinant acidic FGF (aFGF), were used in immunofluorescence studies to localize this growth factor in several normal and dystrophic (mdx) mouse skeletal muscles. The expression of aFGF was detected throughout the life of both the control and mdx mice. In striated muscles, examined up to 3 weeks postnatal, aFGF was localized around the myofibres and this pattern was consistent in both mdx and the normal counterpart strain. However, the intensity of the signal was much stronger in the mdx strain. In mdx mouse skeletal muscles, examined during the acute phase of degeneration and regeneration (3-14 weeks) aFGF was localized around the myofibres, in approximately 60% of the nuclei of newly formed or regenerated myofibres and also in the pockets of necrosis which represented actively degenerating myofibres. In normal mouse skeletal muscles, studied over the same period, the antibodies localized aFGF mainly to the periphery of the muscle fibres. The augmentation of aFGF observed by immunofluorescence in mdx mouse muscles was confirmed by enzyme immunoassay (EIA) analysis of the same muscles over the same period of time. The data from the EIA indicated a 3.5-fold increase in aFGF in mdx as compared to normal muscles at 3 weeks, and an approximate 26-fold increase during the period of active degeneration-regeneration. This increased concentration of aFGF noted in the mdx muscles suggests that this endogenous aFGF may participate in the high level of regenerative activity observed in mdx mouse.
ISSN:0897-7194
DOI:10.3109/08977199209046399
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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2. |
Fibroblast Growth Factor-stimulated Phosphorylation of a Lipocortin I-like Protein is S-Phase Cell Cycle Specific in Human Vascular Endothelial Cells |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 107-116
PatteChristine,
BlanquetPierre R.,
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摘要:
AbstractWe examined whether the phosphorylation of a 34 kDa lipocortin I-like protein may be associated with internalization process of fibroblast growth factor (FGF) in human umbilical vein endothelial (HUVE) cells. We show that: 1) exposure of synchronized HUVE cells to basic FGF for an appreciable time lag (≥30 min) at 37°C and subsequent phosphorylation at 37°C are required to obtain an increased32P-labelling of a 34 kDa substrate; 2) this FGF-stimulated phosphorylation occurs in S phase but not G1 phase of the growth cycle; 3) the 34 kDa substrate appears to be phosphorylated on tyrosine residues; 4) a major fraction of the 34 kDa32P-labelled substrate is immunoprecipitated with an antibody that has been raised against human lipocortin/annexin of type I. It is suggested that internalized FGF-receptor/kinase complexes might be primarily responsible for the phosphorylation of the 34 kDa lipocortin I-related protein in S phase HUVE cells.
ISSN:0897-7194
DOI:10.3109/08977199209046400
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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3. |
Intermolecular Cystine-Bonding of Murine Interleukin 2 Indicates that Ligand Dimerization is Important for the Formation of the High-Affinity Receptor Complex |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 117-129
LotherHeinz,
MütherHorst,
GessnerAndré,
AbdallahSaid,
KüklhlckeKlaus,
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摘要:
AbstractInterleukin 2 is thought to be active as a monomeric protein. As the nonessential Cys-140 of murine interleukin 2 (mIL2) is located in the hydrophobic interface of the amphiphilic F domain it was successfully used to stabilize hydrophobic amino acid contacts between two mIL2 cores yielding biologically active cystine-bonded dimeric mIL2. (3H) thymidine incorporation assays with intermolecular cystine-bonded or monomeric mIL2 revealed almost identical median effective concentrations (EC50) and high-affinity dissociation constants (Kdh), respectively. Comparative binding and internalization assays suggest that one cystine-bonded dimeric or two monomeric mIL2 molecules bind to the high-affinity receptor complex. Furthermore, DSS concentration-dependent crosslinking studies using monomeric mIL2 revealed four membrane-derived protein-complexes with apparent molecular weights of about 70 kDa, 85 kDa, 95 kDa and 100 kDa, respectively, showing that both mIL2 receptor chains may be crosslinked to a monomeric or dimeric ligand molecule, respectively. We therefore propose that dimerization of murine interleukin 2 occurring either in solution at concentrations above the low-affinity dissociation constant or at the low-affinity receptor is important for regulation of high-affinity complex formation and signal transduction.
ISSN:0897-7194
DOI:10.3109/08977199209046401
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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4. |
High Levels of Biologically Active Vascular Endothelial Growth Factor (VEGF) are Produced by the Baculovirus Expression System |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 131-138
CohenTzafra,
GitayHela,
NeufeldGera,
ZionBen,
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摘要:
AbstractVascular endothelial growth factor (VEGF) is a recently discovered mitogen for endothelial cellsin vitro, and a potent angiogenesis promoting factorin vivo.VEGF is secreted from producing cells as a homodimer, binds to specific receptors on the cell surface of endothelial cells, and is produced in four forms as a result of alternative splicing. We have expressed the cDNA encoding the 165 amino-acid long isoform of VEGF in insect cells using the baculovirus based expression vector. We show that infected insect cells secrete large amounts of VEGF. Antibodies directed against a synthetic peptide prepared from human VEGF identify the secreted factor. The baculovirus derived VEGF expressed in insect cells (inVEGF) binds directly to the VEGF receptors, in VEGF competes with pure mammalian cells derived [125I]-VEGF for binding to the VEGF receptors that are present on the cell surface of endothelial cells. Furthermore, inVEGF is biologically active and induces the proliferation of human umbilical vein derived endothelial cells.
ISSN:0897-7194
DOI:10.3109/08977199209046402
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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5. |
Expression and Characterization of Bone Morphogenetic Protein-2 in Chinese Hamster Ovary Cells |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 139-150
IsraelDavid I.,
NoveJohn,
KernsKelvin M.,
MoutsatsosIoannis K.,
KaufmanRandal J.,
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摘要:
AbstractBone is a dynamic tissue that responds to many factors including vitamin D, parathyroid hormone, estrogen, calcitonin, and bone morphogenetic proteins (BMPs). The ability to stimulate new bone growth would permit novel therapies for situations where bone mass has been lost due to accident or disease. Purified BMP-2, in conjunction with a suitable matrix, is sufficient to stimulate the synthesis of new bone (Wang et al., 1990). We have expressed recombinant human BMP-2 at high levels in Chinese hamster ovary cells using methotrexate-mediated gene amplification. Several forms of BMP-2 are secreted from CHO cells: (1) an amino-terminal propeptide of 40-45 kDa, (23) a mature active 30 kDa homodimer consisting of 18-22 kDa subunits, and (3) a small amount of uncleaved 60 kDa precursor protein. The mature, active protein is predominantly a 30 kDa homodimer consisting of subspecies of 18 and 22 kDa which differ by proteolytic processing at their amino termini. Mature BMP-2 and propeptide contain high mannose and complex N-linked oligosaccharides, respectively. The molar amount of secreted, processed propeptide is approximately 5-fold higher than mature BMP-2 in conditioned medium. BMP-2 associates with both the extracellular matrix and the surface of CHO cells, which may in part account for the unequal levels of extracellular propeptide and mature forms of the molecule in the conditioned medium. Recombinant BMP-2 can be expressed in sufficient quantities to assess its therapeutic potential for bone regeneration.
ISSN:0897-7194
DOI:10.3109/08977199209046403
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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6. |
Purification and Biochemical Characterisation of Human and Murine Stem Cell Inhibitors (SCI) |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 151-160
GrahamGerard J.,
FreshneyMary G.,
DonaldsonDebra,
PragnellIan B.,
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摘要:
AbstractWe have recently characterised an inhibitor of haemopoietic stem cell proliferation (SCI/MIP-lα) and report here on its purification and initial biological and biochemical characterisation. The activity can be detected by direct addition to the CFU-A stem cell assay and this simple test for inhibitory activity has greatly facilitated the purification of the molecule. The purification involves a combination of Mono Q ion exchange chromatography, heparin-sepharose affinity chromatography and Blue Sepharose affinity chromatography. The purified stem cell inhibitor is an 8kD peptide which is identical to the previously described peptide macrophage inflammatory protein 1 alpha. The peptide has a natural tendency to form large self-aggregates and appears, in physiological buffers, to have a native molecular weight of around 90kD. SCI is a heat stable, protease sensitive protein which is half maximally active at between 10 and 25pM in the CFU-A assay. The self-aggregates can be disrupted by dilute solutions of acetic acid and it appears that disruption increases the specific activity of SCI preparations. We also report the characterisation of the human homologue of the stem cell inhibitor (human SCI/MIP-1α) which is 74% identical to murine MIP-1 alpha and which shares all the above features of the murine inhibitor.
ISSN:0897-7194
DOI:10.3109/08977199209046404
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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7. |
Modulation of Acute Phase Protein Synthesis in Cultured Rat Hepatocytes by Human Recombinant Hepatocyte Growth Factor |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 161-165
PierzchalskiPiotr,
NakamuraToshikazu,
TakeharaToyohiro,
KojAleksander,
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摘要:
AbstractHuman recombinant hepatocyte growth factor (HGF) added to primary cultures of rat hepatocytes stimulates synthesis of some acute phase proteins, especiallyα-2-macrogobulin. As indicated by changes in mRNA abundance HGF increasesα-2-macroglobulin production at the pretranslational level. Interleukin-6, the main acute-phase cytokine, does not show synergy with HGF in enhancing synthesis ofα-2-macroglobulin, and inhibits HGF-induced DNA-synthesis. On the other hand, dexamethasone potentiates the effects of HGF on synthesis of DNA and acute phase proteins by cultured rat hepatocytes.
ISSN:0897-7194
DOI:10.3109/08977199209046405
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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8. |
Book Review |
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Growth Factors,
Volume 7,
Issue 2,
1992,
Page 167-168
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摘要:
AbstractBeijing Symposium 1991—“Blood Cell Growth Factors: Their Present and Future Use in Hematology and Oncology”(Editor M. J. Murphy, PublisherαAlphaMed Press, Dayton, OH)
ISSN:0897-7194
DOI:10.3109/08977199209046406
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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